A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211733



Internal ID20778773
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:71236171..71245247hg38UCSC Ensembl
chr4:72101888..72110964hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg389077
hg199077
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6387427
Supporting Variants
Samples
Known GenesSLC4A4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211733
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer